FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

STOOL-COLLECTION/PRESERVATION KIT

K Number: K822870 · Decision Nov 1, 1982
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
11
Applicant Total
28
Review Days
35

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Basic Information

Device Name
STOOL-COLLECTION/PRESERVATION KIT
K Number
K822870
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.3250
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
American Scientific Products
Date Received
September 27, 1982
Decision Date
November 1, 1982
Product Code
KDT
Advisory Committee
Pathology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KDT Container, Specimen Mailer And Storage, Sterile

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Other Clearances by American Scientific Products

K Number Device Name
K864824 INFECTIOUS TISSUE KIT
K844042 BLOOD DILUTION VIAL
K831634 GLUCOSE REAGENT B6360-11
K831625 UREA NITROGEN-BUN-REAGENTS B6360-12
K831626 UREA NITROGEN-BUN-REAGENTS B6370-11A
K831628 CREATININE REAGENTS B6370-13
K831624 GLUCOSE REAGENT KITS-B6370-10A
K831627 CREATININE REAGENTS B6360-10
K831569 REAGENT CUPS
K831571 ROTOR
Search all 28 clearances from American Scientific Products →